Clinical Trials Directory

Trials / Completed

CompletedNCT00242606

Lamotrigine Versus Levetiracetam in the Initial Monotherapy of Epilepsy

Lamotrigine Versus Levetiracetam in the Initial Monotherapy of Epilepsy: An Open, Prospective, Multicenter, Randomized Phase III Study

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
409 (actual)
Sponsor
Philipps University Marburg · Academic / Other
Sex
All
Age
12 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to compare the efficacy, safety and tolerance of the drugs Lamotrigine and Levetiracetam in the initial monotherapy of patients with newly diagnosed epilepsy.

Detailed description

Epilepsy is the second most frequent neurologic disease (prevalence 0.5 % - 1 % \[Brodie et al. 1997\]). About 30 % of epilepsy patients (including many children) suffer from intractable seizures \[Kwan \& Brodie 2000\]. Therefore new drugs and an expansion of permission for drugs with limited approval, respectively, are needed. Levetiracetam is a new potent antiepileptic drug with nearly ideal pharmacokinetic properties and few side effects \[Patsalos 2000\], but it is approved in Germany only for add-on therapy for patients \> 15 years of age with focal epilepsy. Due to its few cognitive side effects and its efficacy, Lamotrigine is becoming standard therapy for focal and generalized epilepsy for patients from \>11 years of age. Its disadvantage is the possibility of severe allergic reactions which limits the speed of dose increment. Comparisons: Patients with newly diagnosed epilepsy are treated with either Lamotrigine or Levetiracetam. Rate of seizure-free patients in the first 6 weeks of the trial (main outcome criterion) as well as rate of seizure-free patients during the last 16 weeks and the total 26 weeks of the observation period, time until the first seizure appears, time patients take the study medication, safety and quality of life during treatment are compared.

Conditions

Interventions

TypeNameDescription
DRUGLamotriginetitrate to 200mg over 10 weeks and maintained until end of week 26
DRUGLevetiracetamtitrate to 2000mg/day over 22 days, maintain until the end of week 26

Timeline

Start date
2005-03-01
Primary completion
2008-06-01
Completion
2009-01-01
First posted
2005-10-20
Last updated
2012-05-09

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT00242606. Inclusion in this directory is not an endorsement.